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The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy

✍ Scribed by Henry Houlden; Matilde Laura; Lionel Ginsberg; Heinz Jungbluth; Stephanie A. Robb; Julian Blake; Susan Robinson; Rosalind H.M. King; Mary M. Reilly


Book ID
116793864
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
634 KB
Volume
19
Category
Article
ISSN
0960-8966

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